CN106939166B - A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant - Google Patents
A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant Download PDFInfo
- Publication number
- CN106939166B CN106939166B CN201710155856.XA CN201710155856A CN106939166B CN 106939166 B CN106939166 B CN 106939166B CN 201710155856 A CN201710155856 A CN 201710155856A CN 106939166 B CN106939166 B CN 106939166B
- Authority
- CN
- China
- Prior art keywords
- 2caob
- flame retardant
- prepared
- nanometer
- composite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/02—Inorganic materials
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Fireproofing Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant, the composite flame-retardant agent are by CaCl2、H3BO3, NaOH and Mg (OH)2Nanometer sheet hydro-thermal reaction at 160~200 DEG C is prepared for 6~10 hours.The method of the present invention is simple, of low cost, and low-temperature hydrothermal reaction has prepared 2CaOB by reaction in-situ2O3·H2O load Mg (OH)2Composite nanometer flame retardant, and prepared 2CaOB2O3·H2O/Mg(OH)2Nanometer flame retardent materials good dispersion, grain size are small, and with preferable flame retardant effect and suppression cigarette effect.
Description
Technical field
The invention belongs to field of fire-proof technology, and in particular to a kind of 2CaOB of excellent flame retardancy2O3·H2O/Mg
(OH)2Nanometer flame retardent materials.
Background technology
With fire disaster number increase and plastics burn caused by secondary pollution problems appearance, fire retardant
Using having received widespread attention.Line borate is a kind of highly effective inorganic anti-flaming agent, it have thermal stability height, fine size,
Volume mass is small, easy dispersion, the distinguishing features such as nontoxic, can be fire-retardant but also press down cigarette, and electric arc can be eliminated, therefore have good
Market prospects are widely used in the side such as various fibers, resin, rubber, electrical apparatus insulation material, electric wire, cable, antirust paint
Face it is fire-retardant.
However, the relatively large grain size of line borate is difficult dispersion in matrix, its application industrially is limited；Due to receiving
The pattern and size of rice material have a significant impact to its flame retardant property, and for the fire retardant of equivalent, grain size is cured small specific surface product
It is bigger, after fine, nanosizing, enhance the interaction at interface, can be evenly be scattered in matrix, more effectively
Improve the mechanical property of blend composition, flame retardant effect is just better.Single fire retardant always has the defects of certain in use, such as
Inorganic combustion inhibitor aluminium hydroxide, the magnesium hydroxide being commonly used, during use, the demand to loading is larger.Such as
Nano boric acid salt with other fire retardants is compounded and is used in combination by fruit, can both play the suppression hood of flame retardant synergism and borate,
The dosage of fire retardant can also be reduced.So the preparation of development line borate nano material and its composite flame-retardant agent and flame retardant property are ground
Study carefully and have important practical significance.
Inventor has found that the preparation in relation to being hydrated line borate nanostructured is reported seldom in R＆D process, although
Lihong Bao et al. propose to prepare line borate 2CaOB using hydro-thermal method2O3·H2O nanobelts, and inventor seminar
Once ellipsoid, silkworm chrysalis shape 4CaO5B were reported2O3·7H2The preparation of O nanostructureds, phase inversion prepare sheet, ellipsoid,
Cauliflower-shaped CaO3B2O3·4H2O nanostructureds, but not it is proposed that being 2CaOB about composition2O3·H2The nanoscale of O
Relevant report prepared by compound product.
Invention content
The technical problems to be solved by the invention are to provide a kind of small grain size, good dispersion, excellent flame retardancy
2CaO·B2O3·H2O/Mg(OH)2Composite nanometer flame retardant.
Technical solution is the 2CaOB used by solving above-mentioned technical problem2O3·H2O/Mg(OH)2Nano combined resistance
Combustion agent is prepared by following methods：
By CaCl2、H3BO3, NaOH and Mg (OH)2Nanometer sheet is 1 in molar ratio:1~6:7~10:0.1~0.3 addition is gone
In ionized water, room temperature ultrasonic disperse is uniform, hydro-thermal reaction 6~10 hours, cooled to room temperature, gained at 160~200 DEG C
Product obtains 2CaOB through filtering, washing, drying2O3·H2O/Mg(OH)2Composite nanometer flame retardant.
In above-mentioned preparation method, preferably CaCl2、H3BO3, NaOH and Mg (OH)2Molar ratio be 1:3:7.5:0.2.
In above-mentioned preparation method, hydro-thermal reaction 8 hours further preferably at 180 DEG C.
Above-mentioned Mg (OH)2A length of 100~200nm, the thickness of nanometer sheet are 20~30nm.
The method of the present invention is simple, of low cost, and low-temperature hydrothermal reaction has prepared 2CaOB by reaction in-situ2O3·
H2O load Mg (OH)2Composite nanometer flame retardant, and prepared 2CaOB2O3·H2O/Mg(OH)2Nano composite fire retardant material
Expect that good dispersion, grain size are small, and with preferable flame retardant effect and suppression cigarette effect.
Description of the drawings
Fig. 1 is the X-ray powder diffraction spectrum of sample prepared by embodiment 1.
Fig. 2 is the EDS energy spectrum diagrams of sample prepared by embodiment 1.
Fig. 3 is the SEM figures of sample prepared by embodiment 1.
Fig. 4 is the TEM figures of sample prepared by embodiment 1.
Fig. 5 is Mg (OH)2Nanometer sheet (curve a), 2CaOB2O3·H2O nanobelts (curve b) and 2CaOB2O3·
H2O/Mg(OH)2Composite nanometer flame retardant (the thermogravimetric analysis figure of curve c).
Fig. 6 is the X-ray powder diffraction spectrum of sample prepared by embodiment 2.
Fig. 7 is the SEM figures of sample prepared by embodiment 2.
Fig. 8 is the X-ray powder diffraction spectrum of sample prepared by embodiment 3.
Fig. 9 is the SEM figures of sample prepared by embodiment 3.
Figure 10 is to add 10%Mg (OH) in polypropylene (a) and polypropylene respectively2Nanometer sheet (b), 2CaOB2O3·
H2O nanobelts (c), 2CaOB2O3·H2O and Mg (OH)2Mixture (d), 2CaOB2O3·H2O/Mg(OH)2It is nano combined
The oxygen index value figure of fire retardant (e).
Specific embodiment
The present invention is described in more detail with reference to the accompanying drawings and examples, but protection scope of the present invention is not limited only to
These embodiments.
Mg (OH) used in example below2Nanometer sheet is prepared according to following methods：It is added in three-neck flask
10mL concentrated ammonia liquors, 22mL1.7molL-1MgCl2Aqueous solution and 0.02g cetyl trimethylammonium bromides, 60 DEG C are reacted 75 points
Clock, room temperature are aged 3 hours, products therefrom are filtered, is washed successively with redistilled water and absolute ethyl alcohol, products obtained therefrom is at 60 DEG C
Lower drying 12 hours obtains white powder Mg (OH)2Nanometer sheet.
Embodiment 1
By 0.92g (8mmol) CaCl2、1.48g(24mmol)H3BO3, 2.47g (60mmol) NaOH and 0.1g
(1.6mmol)Mg(OH)2Nanometer sheet is added in 60mL deionized waters, is uniformly mixed, gained mixed solution is placed in ultrasound
In washer in the case where power is 500W, frequency is 60kHz, then room temperature ultrasonic disperse 30 minutes is transferred to volume and gathers for 100mL
In the stainless steel cauldron of tetrafluoroethene liner, reaction kettle is placed in baking oven and keeps the temperature 8 hours for 180 DEG C, reaction kettle is taken out,
Cooled to room temperature in air, products therefrom is through suction filtration, 80 DEG C of redistilled water and absolute ethyl alcohol washing, 60 DEG C of dryings 12
Hour, obtain 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant.
Inventor respectively ties embodiment 1, gained sample using X-ray diffractometer, scanning electron microscope and transmission electron microscope
Structure and morphology characterization, the result is shown in Figure 1~4.As seen from Figure 1, the XRD spectrum of sample contains 2CaOB2O3·H2O and Mg (OH)2
Diffraction maximum, can be seen that in sample containing tetra- kinds of elements of Ca, B, O, Mg from the EDS power spectrums of Fig. 2, so the sample of synthesis can
To be pointed out as 2CaOB2O3·H2O and Mg (OH)2Compound.As can be seen that Mg (OH) from Fig. 3,42Hexagonal nanosheet
(long 100~200nm, thickness about 25nm) deposits 2CaOB formed in situ when with suction-operated2O3·H2O nanobelts
Surface.
Comparative example 1
In embodiment 1, Mg (OH) is not added2Nanometer sheet, other steps are same as Example 1, obtain 2CaO
B2O3·H2O nanobelts.
Inventor is using thermogravimetric analyzer to Mg (OH)22CaOB prepared by nanometer sheet, comparative example 12O3·H2O nanometers
2CaOB prepared by band, embodiment 12O3·H2O/Mg(OH)2Composite nanometer flame retardant carries out thermogravimetric analysis, as a result sees Fig. 5, and three
A sample is shown in Table 1 in 200 DEG C to 600 DEG C of weight loss.
Table 1
Mg (OH) can be calculated by the result of Fig. 5 and table 12In 2CaOB prepared by embodiment 12O3·H2O/Mg
(OH)2Mass fraction in composite nanometer flame retardant is about 19.0%, 2CaOB2O3·H2Mass fraction is about shared by O
81.0%.
Embodiment 2
By 0.92g (8mmol) CaCl2、0.49g(8mmol)H3BO3, 2.24g (56mmol) NaOH and 0.1g
(1.6mmol)Mg(OH)2It adds in 60mL deionized waters, is uniformly mixed, gained mixed solution is placed in ultrasonic cleaning machine
In in the case where power is 500W, frequency is 60kHz, then room temperature ultrasonic disperse 30 minutes is transferred to volume as 100mL polytetrafluoroethylene (PTFE)
In the stainless steel cauldron of liner, reaction kettle is placed in baking oven and keeps the temperature 10 hours for 160 DEG C, reaction kettle is taken out, in air
Cooled to room temperature, products therefrom is through filtering, 80 DEG C of redistilled water and absolute ethyl alcohol washing, 60 DEG C of dryings 12 hours,
Obtain 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant.By Fig. 6 and Fig. 7 as it can be seen that synthesized sample can be referred to
Think 2CaOB2O3·H2O and Mg (OH)2Compound.
Embodiment 3
By 0.92g (8mmol) CaCl2、2.97g(48mmol)H3BO3, 3.20g (80mmol) NaOH and 0.1g
(1.6mmol)Mg(OH)2It adds in 60mL deionized waters, is uniformly mixed, gained mixed solution is placed in ultrasonic cleaning machine
In in the case where power is 500W, frequency is 60kHz, then room temperature ultrasonic disperse 30 minutes is transferred to volume as 100mL polytetrafluoroethylene (PTFE)
In the stainless steel cauldron of liner, reaction kettle is placed in baking oven and keeps the temperature 6 hours for 200 DEG C, reaction kettle is taken out, in air
Cooled to room temperature, products therefrom is through filtering, 80 DEG C of redistilled water and absolute ethyl alcohol washing, 60 DEG C of dryings 12 hours,
Obtain 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant.By Fig. 8 and Fig. 9 as it can be seen that synthesized sample can be referred to
Think 2CaOB2O3·H2O and Mg (OH)2Compound.
In order to prove beneficial effects of the present invention, inventor adds using polypropylene as research object into polypropylene respectively
2CaOB prepared by 10% (polyacrylic mass fraction is 90%) embodiment 12O3·H2O/Mg(OH)2Nano composite fire retardant
Agent, Mg (OH)2Nanometer sheet, 2CaOB2O3·H2O nanobelts and Mg (OH)2And 2CaOB2O3·H2O is with physical mixed side
Formula mixing gained mixture (2CaOB in mixture2O3·H2The mass percentage of O is 81.0%, Mg (OH)2Quality hundred
Divide content 19.0%), then to be carried out using JF-3 oxygen index measurers (the bright thunder experimental instruments and equipment limited in Nanjing provides)
Flame retardant property is tested, the result is shown in Figure 10.The result shows that：2CaOB prepared by the embodiment of the present invention 12O3·H2O/Mg(OH)2It receives
The flame retardant property of rice composite flame-retardant agent is than simple sample and 2CaOB2O3·H2O and Mg (OH)2The flame retardant property of physical mixed
It is good.Due to Mg (OH)22CaOB formed in situ is deposited with suction-operated2O3·H2O nanometers of belt surfaces, the two collaboration
Effect finally improves the flame retardant property of sample.
Claims (3)
1. a kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant, it is characterised in that it is prepared by following methods：
By CaCl2、H3BO3, NaOH and Mg (OH)2Nanometer sheet is 1 in molar ratio:1~6:7~10:0.1~0.3 adds in deionization
In water, room temperature ultrasonic disperse is uniform, hydro-thermal reaction 6~10 hours at 160~200 DEG C, cooled to room temperature, gained production
Object obtains 2CaOB through filtering, washing, drying2O3·H2O/Mg(OH)2Composite nanometer flame retardant, wherein the Mg (OH)2It receives
A length of 100~200 nm, the thickness of rice piece are 20~30 nm.
2. 2CaOB according to claim 12O3·H2O/Mg(OH)2Composite nanometer flame retardant, it is characterised in that：It is described
CaCl2、H3BO3, NaOH and Mg (OH)2Molar ratio be 1:3:7.5:0.2.
3. 2CaOB according to claim 1 or 22O3·H2O/Mg(OH)2Composite nanometer flame retardant, it is characterised in that：
Hydro-thermal reaction 8 hours at 180 DEG C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710155856.XA CN106939166B (en) | 2017-03-16 | 2017-03-16 | A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710155856.XA CN106939166B (en) | 2017-03-16 | 2017-03-16 | A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106939166A CN106939166A (en) | 2017-07-11 |
| CN106939166B true CN106939166B (en) | 2018-07-10 |
Family
ID=59469324
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710155856.XA Expired - Fee Related CN106939166B (en) | 2017-03-16 | 2017-03-16 | A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106939166B (en) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5785939A (en) * | 1995-10-18 | 1998-07-28 | U.S. Borax Inc. | Method for producing calcium borate |
| CN101239725A (en) * | 2008-03-18 | 2008-08-13 | 景德镇陶瓷学院 | Nano-stage calcium borate and use thereof |
| CN103011187B (en) * | 2012-12-14 | 2014-12-03 | 陕西师范大学 | Preparation method of nano-sized CaO.3 B2o3.4 H2O |
| CN106185969B (en) * | 2016-07-14 | 2018-03-06 | 陕西师范大学 | A kind of 2MgOB2O3·1.5H2The preparation method of O nanometer stubs |
-
2017
- 2017-03-16 CN CN201710155856.XA patent/CN106939166B/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN106939166A (en) | 2017-07-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Shao et al. | A strategy to construct multifunctional ammonium polyphosphate for epoxy resin with simultaneously high fire safety and mechanical properties | |
| Wang et al. | Constructing hierarchical structure based on LDH anchored boron-doped g-C3N4 assembled with MnO2 nanosheets towards reducing toxicants generation and fire hazard of epoxy resin | |
| Wang et al. | Designing hierarchical ternary structure based on NiAl LDH anchored phosphorus-doped g-C3N4 dotted with Fe3O4 nanoparticles towards improving the fire safety of thermoplastic polyurethane | |
| Peng et al. | Amorphous cobalt borate nanosheets grown on MoS2 nanosheet for simultaneously improving the flame retardancy and mechanical properties of polyacrylonitrile composite fiber | |
| Shi et al. | Sodium alginate-templated synthesis of g-C3N4/carbon spheres/Cu ternary nanohybrids for fire safety application | |
| CN102408581B (en) | Attapulgite/hydrotalcite compound flame retardant material and preparation method thereof | |
| Oualha et al. | Development of metal hydroxide nanoparticles from eggshell waste and seawater and their application as flame retardants for ethylene-vinyl acetate copolymer (EVA) | |
| Jin et al. | Intercalation of organic and inorganic anions into layered double hydroxides for polymer flame retardancy | |
| Yan et al. | Novel bio-derived phytic acid and melamine interlayered/surface dual modified layered double hydroxide by one-pot method and its highly efficient flame retardant performance for polypropylene | |
| Xu et al. | Nickel hydroxide and zinc hydroxystannate dual modified graphite carbon nitride for the flame retardancy and smoke suppression of epoxy resin | |
| CN109517220A (en) | A kind of preparation method of nanometer of tinbase expanding fire retardant | |
| CN104893248A (en) | Preparation method and application of inorganic hybrid smoke-suppression flame retardant | |
| Wang et al. | Effect of modified hydrotalcites on flame retardancy and physical properties of paper | |
| Du et al. | Flame retardancy of organic-anion-intercalated layered double hydroxides in ethylene vinyl acetate copolymer | |
| CN108622921A (en) | A kind of high temperature resistant low-sodium aluminum hydroxide novel preparation method | |
| CN106939166B (en) | A kind of 2CaOB2O3·H2O/Mg(OH)2Composite nanometer flame retardant | |
| Cui et al. | Synergistic effects of layered double hydroxide with phosphorus-nitrogen intumescent flame retardant in PP/EPDM/IFR/LDH nanocomposites | |
| CN103011187B (en) | Preparation method of nano-sized CaO.3 B2o3.4 H2O | |
| CN103408960B (en) | Lanthanum stannate and application of composition of lanthanum stannate and inorganic flame retardant in halogen-containing superpolymer | |
| Sun et al. | A novel and convenient zeolite modification strategy for enhancing the fire resistance of epoxy resin | |
| CN106904627B (en) | 2MgO·B2O3·1.5H2O/Mg(OH)2Nanometer flame retardent materials and its in-situ preparation method | |
| Wang et al. | The synergistic effect of lamellar cobalt phosphate and sodium metaborate hydrate improves the flame retardancy of epoxy resin | |
| CN110627079B (en) | Ternary borate hydrotalcite flame retardant and preparation method and application thereof | |
| CN101519509A (en) | Magnesium hydrate powder coated by inorganic compound as well as preparation method and application of same | |
| Gao et al. | Flame retardancy and mechanical properties of a novel zinc hydroxystannate/epoxy resin nanocomposite |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20180710 Termination date: 20210316 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |